Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Recruiting Not applicable Interventional

Staged Complete Revascularization for Coronary Artery Disease vs Medical Management Alone in Patients With AS Undergoing Transcatheter Aortic Valve Replacement

ClinicalTrials.gov ID: NCT04634240

Public ClinicalTrials.gov record NCT04634240. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 2:24 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Comparative Effectiveness Study of Staged Complete Revascularization With Percutaneous Coronary Intervention to Treat Coronary Artery Disease vs Medical Management Alone in Patients With Symptomatic Aortic Valve Stenosis Undergoing Elective Transfemoral Transcatheter Aortic Valve Replacement: The COMPLETE TAVR Study

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Patients undergoing transcatheter aortic valve replacement (TAVR) often have concomitant coronary artery disease (CAD) which may adversely affect prognosis. There is uncertainty about the benefits and the optimal timing of revascularization for such patients. There is currently clinical equipoise regarding the management of concomitant CAD in patients undergoing TAVR. Some centers perform routine revascularization with percutaneous coronary intervention (PCI) (either before or after TAVR), while others follow an alternative strategy of medical management. The potential benefits and optimal timing of PCI in these patients are unknown. As TAVR expands to lower risk patients, and potentially becomes the preferred therapy for the majority of patients with severe aortic stenosis, the optimal management of concomitant coronary artery disease will be of increasing importance. The COMPLETE TAVR study will determine whether, on a background of guideline-directed medical therapy, a strategy of complete revascularization involving staged PCI using drug eluting stents to treat all suitable coronary artery lesions is superior to a strategy of medical therapy alone in reducing the composite outcome of Cardiovascular Death, new Myocardial Infarction, Ischemia-driven Revascularization or Hospitalization for Unstable Angina or Heart Failure. The study will be a randomized, multicenter, open-label trial with blinded adjudication of outcomes. Patients will be screened and consented for elective transfemoral TAVR and randomized within 96 hours of successful balloon expandable TAVR. Complete Revascularization: Staged PCI using third generation drug eluting stents to treat all suitable coronary artery lesions in vessels that are at least 2.5 mm in diameter and that are amenable to treatment with PCI and have a ≥70% visual angiographic diameter stenosis. Staged PCI can occur any time from 1 to 45 days post successful transfemoral TAVR. Vs. Medical Therapy Alone: No further revascularization of coronary artery lesions. All patients, regardless of randomized treatment allocation, will receive guideline-directed medical therapy consisting of risk factor modification and use of evidence-based therapies. The COMPLETE TAVR study will help address the current lack of evidence in this area. It will likely impact both the global delivery of health care and the management and clinical outcomes of all patients undergoing TAVR with concomitant CAD.

Study identification

NCT ID
NCT04634240
Recruitment status
Recruiting
Study type
Interventional
Phase
Not applicable
Enrollment
4,000 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Not listed
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 18, 2020
Primary completion
Mar 31, 2026
Completion
Mar 31, 2026
Last update posted
Jul 23, 2025

2020 – 2026

United States locations

U.S. sites
55
U.S. states
26
U.S. cities
52
Facility City State ZIP Site status
Huntsville Heart Center Huntsville Alabama 35801 Recruiting
Arizona Cardiovascular Research Phoenix Arizona 85027 Recruiting
Veteran Affairs Palo Alto Health Care System Palo Alto California 94304 Recruiting
Loma Linda University Redlands California 92373 Recruiting
Santa Barbara Cottage Hospital Santa Barbara California 93105 Recruiting
Torrance Memorial Medical Center Torrance California 90505 Recruiting
JFK Medical Center Atlantis Florida 33462 Recruiting
Baptist Health Jacksonville Jacksonville Florida 32207 Recruiting
Miami Cardiac and Vascular/Baptist Hospital Miami Florida 33139 Recruiting
Piedmont Atlanta Georgia 30309 Recruiting
Northeast Georgia Health System Gainesville Georgia 30501 Recruiting
St. Alphonsus Regional Medical Center Boise Idaho 83709 Recruiting
Ascension Alexian Brothers Chicago Illinois 60007 Recruiting
Midwest Cardiovascular Research and Education Foundation Elkhart Indiana 46514 Recruiting
Parkview Research Center Fort Wayne Indiana 46845 Recruiting
University of Kansas Medical Center Kansas City Kansas 66160 Recruiting
Midwest Heart and Vascular Overland Park Kansas 66211 Recruiting
Cardiovascular Research Institute of Kansas Wichita Kansas 64131 Recruiting
Tufts Medical Boston Massachusetts 02111 Recruiting
Massachusetts General Hospital Boston Massachusetts 02114 Recruiting
Sparrow Clinical Research Institute Lansing Michigan 48912 Recruiting
William Beaumont Hospital Royal Oak Michigan 48073 Recruiting
Ascension St. Mary's Saginaw Michigan 48197 Recruiting
St. Joseph Mercy Health System Ypsilanti Michigan 48197 Recruiting
University of Minnesota Medical Center Minneapolis Minnesota 55455 Recruiting
CentraCare Heart and Vascular Center Saint Cloud Minnesota 56303 Recruiting
Boone Hospital Columbia Missouri 65201 Recruiting
St. Louis University St Louis Missouri 63103 Recruiting
Missouri Baptist St Louis Missouri 63131 Recruiting
Bryan Heart Lincoln Nebraska 68506 Recruiting
Dartmouth Hitchcock Medical Center Lebanon New Hampshire 03765 Recruiting
Our Lady of Lourdes Camden New Jersey 08103 Recruiting
Valley Hospital Ridgewood New Jersey 07450 Recruiting
University at Buffalo Buffalo New York 14203 Recruiting
NYU Langone Hospital - Long Island Mineola New York 11501 Recruiting
Mount Sinai New York New York 10029 Recruiting
Columbia University Medical Center New York New York 10552 Recruiting
St. Joseph's Hospital Syracuse New York 13088 Recruiting
Montefiore Medical Center The Bronx New York 10467 Recruiting
Novant Health Heart and Vascular Institute Charlotte North Carolina 28204 Recruiting
Summa Health System Akron Ohio 44304 Recruiting
Mount Carmel Columbus Ohio 43213 Recruiting
Oklahoma Heart Oklahoma City Oklahoma 73110 Recruiting
Kaiser Permanente Northwest Clackamas Oregon 97015 Recruiting
Rhode Island Hospital Providence Rhode Island 02903 Recruiting
Methodist Le Bonheur Healthcare Germantown Tennessee 38138 Recruiting
Ballad Health CVA Heart Institute Kingsport Tennessee 37660 Recruiting
Parkwest Medical Center Knoxville Tennessee 37923 Recruiting
Cardiovascular Surgery Clinic/Baptist Memorial Memphis Tennessee 38671 Recruiting
HCA Houston Healthcare Medical Center Houston Texas 77004 Recruiting
Baylor Scott & White Plano Plano Texas 75093 Recruiting
Baylor Scott & White Round Rock Round Rock Texas 78665 Recruiting
University of Vermont Medical Center Burlington Vermont 05401 Recruiting
Bellin Health System Green Bay Wisconsin 54301 Recruiting
Ascension Columbia St. Mary's Milwaukee Wisconsin 53211 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04634240, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 23, 2025 · Synced Sep 5, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04634240 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →